Supplementation with a selective amino acid formula ameliorates muscular dystrophy in mdx mice-Reference-Cited by-同舟云学术

Supplementation with a selective amino acid formula ameliorates muscular dystrophy in mdx mice

Published:2018-10-02 Issue:1 Volume:8 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Banfi Stefania,D’Antona Giuseppe,Ruocco Chiara,Meregalli Mirella,Belicchi Marzia,Bella Pamela,Erratico Silvia,Donato Elisa^ORCID,Rossi Fabio,Bifari Francesco^ORCID,Lonati Caterina,Campaner Stefano,Nisoli Enzo^ORCID,Torrente Yvan

Funder

Fondazione Cariplo

Professional Dietetics

Associazione Centro Dino Ferrari

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-018-32613-w.pdf

Reference82 articles.

1. Emery, A. E. The muscular dystrophies. Bmj 317, 991–995 (1998).

2. Davies, K. E. & Nowak, K. J. Molecular mechanisms of muscular dystrophies: old and new players. Nat Rev Mol Cell Biol 7, 762–773 (2006).

3. Grounds, M. D., Radley, H. G., Lynch, G. S., Nagaraju, K. & De Luca, A. Towards developing standard operating procedures for pre-clinical testing in the mdx mouse model of Duchenne muscular dystrophy. Neurobiology of disease 31, 1–19, https://doi.org/10.1016/j.nbd.2008.03.008 (2008).

4. Cerletti, M. et al. Dystrophic phenotype of canine X-linked muscular dystrophy is mitigated by adenovirus-mediated utrophin gene transfer. Gene therapy 10, 750–757, https://doi.org/10.1038/sj.gt.3301941 (2003).

5. Deconinck, A. E. et al. Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy. Cell 90, 717–727 (1997).

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